3-Benzylpyrrolidine → 6-(3-benzylpyrrolidin-1-yl)-N-(3-methylbutyl)pyridazine-3-carboxamide
Reaction equation
Cl[C:2]1[N:7]=[N:6][C:5]([C:8]([NH:10][CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])=[O:9])=[CH:4][CH:3]=1.[CH2:16]([CH:23]1[CH2:27][CH2:26][NH:25][CH2:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH2:16]([CH:23]1[CH2:27][CH2:26][N:25]([C:2]2[N:7]=[N:6][C:5]([C:8]([NH:10][CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])=[O:9])=[CH:4][CH:3]=2)[CH2:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Participants
3
Procedure
The title compound was prepared in the same manner as described for Example 16 from 6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamide and 3-benzylpyrrolidine. MS (+ESI) m/z 353 (MH+).
Sources & evidence
- ORD record
- ord-ef0f28f96f864b05bd905b41667f9a2d
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07799787B2
Reaction notes
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